ClinVar Miner

Submissions for variant NM_152713.5(STT3A):c.509-15G>T

gnomAD frequency: 0.00048  dbSNP: rs185338981
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001720196 SCV000524696 likely benign not provided 2018-06-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001720196 SCV002390963 benign not provided 2024-01-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001720196 SCV005215434 likely benign not provided criteria provided, single submitter not provided

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